{
  "meta": {
    "disclaimer": "Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. We may limit or otherwise restrict your access to the API in line with our Terms of Service.",
    "terms": "https://open.fda.gov/terms/",
    "license": "https://open.fda.gov/license/",
    "last_updated": "2026-08-13",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "cfres_id": "104678",
      "product_res_number": "Z-0135-2012",
      "event_date_initiated": "2011-10-12",
      "event_date_posted": "2011-10-28",
      "recall_status": "Terminated",
      "event_date_terminated": "2012-08-30",
      "res_event_number": "60175",
      "product_code": "FFX",
      "k_numbers": [
        "K031169"
      ],
      "product_description": "AR ManoShield, MSS-3599, 10 pack.\n\nFGS:  MSS-3599,\nIndividual package label: LBL-110275-03,\nBox label: LBL-110282-03,\nPackage Inserts: DOC-3682,\nUser Manual: DOC-1332-12.\n\nProduct Usage:  The MVS disposable sheath (a.k.a. ManoShield) for the high-resolution MVS catheter is designed to provide a biocompatible barrier between the catheter and patient.",
      "code_info": "F1112702UA, F1113101UA, F1113103UA, F1113104UA, F1113401UA, F1114201UA, F1114617UA, F1114618UA, F1114619UA, F1114620UA, F1114621UA, F1114623UA, F1114624UA, F1114625UA, F1114626UA, F1114627UA, F1114628UA, F1114629UA, F1115402UA, F1116306UA, F1117207UA, F1119201UA, F1119401UA, F1121304UA, F1123201UA, F1123405UA, F1123703UA, F1124202UA, F1124301UA, F1125105UA, F1125201UA, F1127303UA, F1128101UA, F1129701UA, F1130202UA, F1130304UA, F1128301UA, F1127103UA, F1127205UA,",
      "firm_fei_number": "3005344223",
      "recalling_firm": "Sierra Scientific Instruments Inc",
      "address_1": "5757 W Century Blvd Ste 660 5757 W Century Blvd",
      "address_2": "Ste 660",
      "city": "Los Angeles",
      "state": "CA",
      "postal_code": "90045-6456",
      "additional_info_contact": "310-641-8492",
      "reason_for_recall": "The recall was initiated after Given Imaging received a test report during a Canadian licensing process where the AR ManoShield exhibited pinholes and did not pass the test, the Field Safety Corrective Action (FSCA) Committee was convened.  As a result of the data discussed during this meeting, a decision was made to voluntarily recall this product, and cease its further commercialization or distr",
      "root_cause_description": "Nonconforming Material/Component",
      "action": "Given Imaging sent an \"Urgent Product Recall 1st Notice\" letter with an attached Device Recall Confirmation Form (via Fed Ex with signature for tracking purposes) to all customers who purchased the AR ManoShield, part numbers MSS-3599.  The letter provides the customers with an explanation of the problem identified and actions to be taken.  Customers were instructed to locate the affected product and removed from use immediately.  The letter stated that if the affected product have been further distributed, forward this letter immediately to all customers who received the affected product.   Customers were asked to complete and return the enclosed confirmation form as per the instructions.  Customers with any questions were instructed to contact Karla Guerrero at (310) 641-8492 ext. 2138 or email at karla.guerrero@givenimaging.com.",
      "product_quantity": "292 units",
      "distribution_pattern": "Worldwide Distribution - USA (nationwide) and the countries of: Austria, Belgium, Canada, Chile, China, Columbia, Ecuador, France, Germany, Israel, Mexico, Poland, Portugal, Sweden, and Switzerland.",
      "openfda": {
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        "registration_number": [
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        ],
        "device_name": "System, Gastrointestinal Motility (Electrical)",
        "medical_specialty_description": "Gastroenterology, Urology",
        "regulation_number": "876.1725",
        "device_class": "2"
      }
    }
  ]
}